Safety and Efficacy of Long-Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open-Label Extension Study

被引:6
作者
Jankovic, Joseph [1 ,2 ]
Coffey, Barbara [3 ]
Claassen, Daniel O. [4 ]
Jimenez-Shahed, Joohi [5 ,6 ]
Gertz, Barry J. [7 ]
Garofalo, Elizabeth A. [7 ]
Stamler, David A. [8 ]
Wieman, Maria [9 ]
Savola, Juha-Matti [10 ]
Harary, Eran [11 ]
Alexander, Jessica [12 ]
Barkay, Hadas [11 ]
Gordon, Mark Forrest [13 ]
机构
[1] Baylor Coll Med, Parkinsons Dis Ctr, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Neurol, Movement Disorders Clin, Houston, TX 77030 USA
[3] Univ Miami, Miller Sch Med, Dept Psychiat & Behav Sci Child & Adolescent Psyc, Miami, FL 33136 USA
[4] Vanderbilt Univ, Div Behav & Cognit Neurol, Dept Neurol, Med Ctr, Nashville, TN USA
[5] Icahn Sch Med Mt Sinai, Movement Disorders Neuromodulat & Brain Circuit, Dept Neurol, New York, NY USA
[6] Icahn Sch Med Mt Sinai, Movement Disorders Neuromodulat & Brain Circuit, Dept Neurosurg, New York, NY USA
[7] Nuvelution TS Pharma Inc, San Francisco, CA USA
[8] Teva Branded Pharmaceut Prod R&D Inc, La Jolla, CA USA
[9] Teva Branded Pharmaceut Prod R&D Inc, W Chester, PA USA
[10] Teva Pharmaceut Int GmbH, Basel, Switzerland
[11] Teva Pharmaceut Ind Ltd, Innovat Med Global Clin Dev, Netanya, Israel
[12] Teva Branded Pharmaceut Prod R&D Inc, Global Med Affairs, W Chester, PA USA
[13] Teva Branded Pharmaceut Prod R&D Inc, Innovat Med Global Clin Dev, W Chester, PA USA
来源
MOVEMENT DISORDERS CLINICAL PRACTICE | 2023年 / 10卷 / 09期
关键词
deutetrabenazine; Tourette syndrome; adolescents; children; VMAT2; SEVERITY; PREVALENCE; PEOPLE;
D O I
10.1002/mdc3.13849
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Tourette syndrome (TS) is a neurodevelopmental disorder characterized by motor and phonic tics. Objective: To assess the safety and efficacy of deutetrabenazine (Teva Neuroscience, Inc, Parsippany, NJ), a vesicular monoamine transporter 2 inhibitor, in children and adolescents with TS. Methods: Alternatives for Reducing Tics in TS (ARTISTS) open-label extension (OLE) (NCT03567291) was a 54-week, global, phase 3, open-label extension study of deutetrabenazine (6-48mg daily) conducted May 28, 2018 to April 3, 2020 with a 2-week randomized withdrawal period. Participants (6-16years of age) had TS and active tics causing distress or impairment. Safety (primary outcome) was assessed by treatment-emergent adverse events (TEAEs) and clinical laboratory testing. Efficacy was measured by the Yale Global Tic Severity Scale-Total Tic Score (YGTSS-TTS). Results: The intent-to-treat population (228 participants; mean age, 12.0years; 79.8% male; 86.4% white) had a median (range) duration of exposure of 28.4 (0.3-52.9) weeks. Of 227 participants in the safety analysis, 161 (70.9%) reported >= 1 TEAE (exposure-adjusted incidence rate, 2.77/patient-year), of which 95 (41.9%) were treatment related. The most frequently reported TEAEs were headaches, somnolence, nasopharyngitis, weight increases, and anxiety. No additional safety signals were observed. Worsening of YGTSS-TTS after the 2-week randomized withdrawal was not statistically significant (least squares mean difference, -0.4; P=0.78). Several exploratory measures showed sustained improvement throughout the treatment periods. Conclusions: In this long-term, open-label trial, deutetrabenazine was well tolerated with low frequency of TEAEs. There was no significant difference in tics between treatment arms during the 2-week randomized withdrawal period, however, descriptive statistics and comparison with baseline showed a numeric improvement in tics, quality of life, and other measures.
引用
收藏
页码:1388 / 1398
页数:11
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